Variant #0000979924 (NC_000011.9:g.824439G>A, NM_173584.3:c.-3651G>A (EFCAB4A))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.824439G>A
DNA change (hg38) -
Published as PNPLA2(NM_020376.4):c.1175+3G>A
ISCN -
DB-ID EFCAB4A_000025
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPLP2 NM_001004.3 -?/. - c.*11603G>A r.(=) p.(=)
PNPLA2 NM_020376.3 -?/. - c.1175+3G>A r.spl? p.?
EFCAB4A NM_173584.3 -?/. - c.-3651G>A r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.